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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848925Generated: October 25, 2026

Dichlorofluoromethane → 1-Butyl-2-chloro-1-ethoxy-2-fluorocyclopropane

https://huagongshe.com/reaction/848925

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichlorofluoromethaneHCID 6370—
ReactantPotassium HydroxideHCID 14797—
Reactant18-Crown-6HCID 28557—
Reactant1-Hexene, 2-ethoxy-HCID 10376321—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product1-Butyl-2-chloro-1-ethoxy-2-fluorocyclopropaneHCID 12786235—

Reaction Conditions

Temperature20 °C

Reaction Steps

To a solution of 61.0 g. of 2-ethoxy-1-hexene, 135 ml. of 13.5 M potassium hydroxide and 217 g. of "18-crown -6" ether at -15° C. is added dropwise over 30 minutes at 0°, a 90 ml. portion of dichlorofluoromethane. After the addition, the mixture is placed in an ice bath. An exotherm raises the temperature to 20° C., whereupon the mixture is placed in a dry-ice/carbon tetrachloride bath to maintain the temperature at -5° C. to 0° C. After three hours at this temperature, the reaction mixture is diluted with water and extracted with ether. The ether extracts are combined, washed with water, then brine, dried over potassium carbonate and concentrated in vacuo to an oil. This oil is distilled through a 6 inch Vigreux column to provide 82 g. of the desired compound as a colorless liquid, b.p. 70°-71° C., 16 mm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04297516
Source datasetuspto-grants-1981_10
ORD IDord-64a44d5f3cc143a290d2f0f98e68c855
Source noteuspto-grants-1981_10